TENS device-HeadaTerm, eEspress
K-Number: K172450 · 2018-09-13
Decision Date2018-09-13
Product CodePCC
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
TENS device-HeadaTerm, eEspress is a medical device manufactured by Wat Medical Technology (Ningbo) Co., Ltd.. It received FDA 510(k) clearance on 2018-09-13 under approval number K172450. The device is classified under product code PCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TENS device-HeadaTerm, eEspress?
TENS device-HeadaTerm, eEspress is a medical device that received FDA 510(k) clearance on 2018-09-13. It is manufactured by Wat Medical Technology (Ningbo) Co., Ltd.. The 510(k) number is K172450.
When was TENS device-HeadaTerm, eEspress approved by the FDA?
TENS device-HeadaTerm, eEspress received FDA 510(k) clearance on 2018-09-13, under approval number K172450.
What company makes TENS device-HeadaTerm, eEspress?
TENS device-HeadaTerm, eEspress is manufactured by Wat Medical Technology (Ningbo) Co., Ltd..
What is the FDA product code for TENS device-HeadaTerm, eEspress?
The FDA product code for TENS device-HeadaTerm, eEspress is PCC.
Other Devices by Wat Medical Technology (Ningbo) Co., Ltd.
Related Devices (Code: PCC)
Official Source
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